- Medtronic (Lafayette, CO)
- …systems engineers and designers in the definition, development, and support of complex medical device systems used to support airway management and intubation. ... and executing tasks for entire projects. + Demonstrate understanding of medical product development, device requirements, regulations, and standards; provide… more
- Medtronic (Lafayette, CO)
- …- Provides expertise in interpreting and implementing regulatory requirements, including medical device directives, FDA regulations, and international standards; ... tools (FMEA, FTA, PHA, ISO 14971) + Knowledge of medical device regulations: FDA 21 CFR Part...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Northridge, CA)
- …compliance, antitrust, privacy, and industry-specific issues relevant to transactions in the medical device and healthcare sectors. + Providing legal guidance ... well as in-house counsel roles + Familiarity with healthcare, medical device , life sciences, or other highly...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Northridge, CA)
- …and sourcing policies. + Familiarity with security and privacy regulations in the medical device or a highly regulated industry. + Highly self-motivated and ... a week. + Experience working in highly regulated industry ( medical device , pharmaceutical, or life sciences industries...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Northridge, CA)
- …IT leadership within life sciences, with at least 5 years specifically in medical device or pharmaceutical regulated settings, including direct support for ... and compliance. + Proven hands-on technical leadership within a medical device company. + Exposure to advanced...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Medtronic (Mounds View, MN)
- …with deep knowledge of ISO 14971 to lead risk management strategy for our medical device products (Capital and disposable). This role is pivotal in ensuring ... Experience in Quality Assurance, Engineering, Capital equipment + **Industry Experience:** Medical device industry. + **Technical Skills:** Proficient in quality… more
- Medtronic (North Haven, CT)
- …to Have** + Bachelor's degree in biomedical engineering. + Test Engineering experience in the medical device industry. + Experience in medical device ... physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully… more
- Medtronic (Boston, MA)
- …multiple teams to execute concurrent, interdependent projects. + Knowledge of medical device R&D, product development, and clinical/regulatory procedures; ... as a Subject Matter Expert + Comprehensive knowledge of medical device standards and regulations (eg, IEC...within the Responsibilities section of this job description are representative of those that must be met by an… more
- Fujifilm (Annapolis, MD)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... - St. Louis/ Southern Illinois) is responsible for the generation of sales revenue for the organization through personal interaction with prospective customers… more
- Medtronic (Oklahoma City, OK)
- …and resolve gaps. + Experience working in a regulated environment--ideally the medical device industry. + Proactively drives results. **Physical Job ... acts as a district liaison for inventory topics between field-based employees ( Sales Reps, Clinical Specialist, District Managers)/ Customers and the internal team… more